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EGFR-IN-97(compound 6q)作为一种EGFR抑制剂,对Ba/F3-EGFRL858R/T790M/C797S和Ba/F3-EGFRDel19/T790M/C797S细胞展示了显著的抑制效果,IC50值分别为0.42 μM和0.41 μM。此外,该化合物在0.8 μM浓度下能有效促进NCI-H1975-EGFRL858R/T790M/C797S细胞的凋亡(apoptosis)。
EGFR-IN-97(compound 6q)作为一种EGFR抑制剂,对Ba/F3-EGFRL858R/T790M/C797S和Ba/F3-EGFRDel19/T790M/C797S细胞展示了显著的抑制效果,IC50值分别为0.42 μM和0.41 μM。此外,该化合物在0.8 μM浓度下能有效促进NCI-H1975-EGFRL858R/T790M/C797S细胞的凋亡(apoptosis)。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
10 mg | 询价 | 10-14周 | |
50 mg | 询价 | 10-14周 |
产品描述 | EGFR-IN-97 (compound 6q), an EGFR inhibitor, demonstrates effectiveness in inhibiting Ba/F3-EGFR L858R/T790M/C797S and Ba/F3-EGFR Del19/T790M/C797S cells, exhibiting IC 50 values of 0.42 μM and 0.41 μM, respectively. Additionally, at a concentration of 0.8 μM, EGFR-IN-97 is capable of inducing apoptosis in NCI-H1975-EGFR L858R/T790M/C797S cells [1]. |
体外活性 | EGFR-IN-97 (compound 6q) 在靶向突变型NSCLC细胞系NCI-H1975-EGFR L858R/T790M/C797S 中表现出卓越的抑制活性,其IC 50 值仅为0.82 μM。该表现优于osimertinib (IC 50 = 2.94 μM)、JBJ-04-125-02 (IC 50 = 3.66 μM),以及JBJ-04-125-02 与osimertinib的联合应用 (IC 50 = 1.25 μM) [1]。 |
分子量 | 624.73 |
分子式 | C37H36N8O2 |
CAS No. | 3020681-05-1 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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